Luboldt H J, Bex A, Swoboda A, Hüsing J, Rübben H
Department of Urology, Biometry and Epidemiology, Universitätsklinikum der Gesamthochschule Essen, Germany.
Eur Urol. 2001 Feb;39(2):131-7. doi: 10.1159/000052427.
While international screening studies for prostate cancer are by now almost reaching the estimated number of recruitments mandatory for the necessary power to investigate an effect on mortality of prostate cancer, no statistical figures on the detection of prostate cancer in Germany - apart from historical data before the use of prostate-specific antigen (PSA) are available. In order to generate a database and to investigate the diagnostic efficacy of the primarily practice-based urological care system, a case finding study designed as a nationwide longitudinal early detection trial was initiated.
In one week in November 1997, 963 urologists prospectively examined 11,644 men between 45 and 75 years of age by digital rectal examination (DRE) and PSA with 4.0 ng/ml as cutoff. Data of family history and physical examination were collected by questionnaire. At this time participants were not aware of their PSA value. PSA was determined in the study center. Indication for sextant biopsy was a PSA value above 4.0 ng/ml or a suspicious lesion on DRE. Any indicated biopsy not performed had to be clarified. In a second questionnaire results of prostate biopsy, treatment and tumor status were documented.
The mean age of the study population was 62 years (median 62). The PSA median was 1.4 ng/ml with 82.8% presenting with < 4.0 ng/ml, 12.8% with 4-10 ng/ml and 4.4% with >10 ng/ml. From 1,115 men (47.7%) biopsied, 262 cancers were detected resulting in a detection rate of 23.5%. While 399 men refused biopsy, further investigation was not recommended in 387 men by their urologist, because prostatitis or benign hyperplasia was thought to be the cause for elevated PSA. From the 143 patients undergoing radical prostatectomy, 93 (65%) cancers were organ confined. T(1c) cancers with elevated PSA > 10 ng/ml could be treated with curative intent in 44% only. The positive predictive value (PPV) was estimated to be 16% for DRE alone (14/90), 17% for PSA alone (143/819) and 51% for the combination of both (105/206). In that cohort, use of age-adjusted PSA values and PSA density increased the PPV of PSA testing nonsignificantly.
Significant higher PPV indicated that utilizing a combination of both DRE and PSA is most effective in the early detection of prostate cancer. Unnecessary biopsies can be avoided using either age-adjusted PSA value or PSA density, but the PPV is not significantly changed and potentially curable cancer is missed in up to 25%. Given the substantial variability of the diagnostic approach despite the study design, uniform guidelines are necessary to ensure countrywide sufficient screening.
虽然目前国际上针对前列腺癌的筛查研究几乎已达到调查前列腺癌对死亡率影响所需效力的估计招募人数,但除了使用前列腺特异性抗原(PSA)之前的历史数据外,德国尚无关于前列腺癌检测的统计数据。为了建立一个数据库并研究以基层医疗为主的泌尿外科护理系统的诊断效力,启动了一项作为全国纵向早期检测试验设计的病例发现研究。
1997年11月的一周内,963名泌尿科医生对11644名45至75岁男性进行了前瞻性检查,采用直肠指检(DRE)和以4.0 ng/ml为临界值的PSA检测。通过问卷收集家族史和体格检查数据。此时参与者不知道自己的PSA值。PSA在研究中心测定。 sextant活检的指征是PSA值高于4.0 ng/ml或DRE发现可疑病变。任何未进行的指示性活检都必须予以说明。在第二份问卷中记录了前列腺活检、治疗和肿瘤状态的结果。
研究人群的平均年龄为62岁(中位数62岁)。PSA中位数为1.4 ng/ml,82.8%的人PSA值<4.0 ng/ml,12.8%的人PSA值为4 - 10 ng/ml,4.4%的人PSA值>10 ng/ml。在1115名接受活检的男性(47.7%)中,检测到262例癌症,检出率为23.5%。虽然有399名男性拒绝活检,但泌尿科医生对387名男性不建议进一步检查,因为认为前列腺炎或良性增生是PSA升高的原因。在143例接受根治性前列腺切除术的患者中,93例(65%)癌症局限于器官内。PSA>10 ng/ml的T(1c)期癌症只有44%可进行根治性治疗。单独DRE的阳性预测值(PPV)估计为16%(14/90),单独PSA的PPV为17%(143/819),两者联合的PPV为51%(105/206)。在该队列中,使用年龄校正后的PSA值和PSA密度对PSA检测的PPV无显著增加。
显著更高的PPV表明,DRE和PSA联合使用在前列腺癌早期检测中最有效。使用年龄校正后的PSA值或PSA密度可避免不必要的活检,但PPV没有显著变化,高达25%的潜在可治愈癌症可能会被漏诊。鉴于尽管有研究设计,但诊断方法存在很大差异,需要统一的指南以确保全国范围内充分的筛查。